小波变换及滚球算法在单分子荧光能量共振转移图像分析中的应用

单分子荧光共振能量转移技术是通过检测单个分子内的荧光供体及受体间荧光能量转移的效率来研究分子构象的变化．要得到这些生物大分子的信息就需要对大量的单分子信号进行统计分析,人工分析这些信息,既费时费力又不具备客观性和可重复性,因此本文将小波变换及滚球算法应用到单分子荧光能量共振转移图像中对单分子信号进行统计分析．在保证准确检测到单分子信号的前提下,文章对滚球算法和小波变换算法处理图像后的线性进行了分析,结果表明,滚球算法和小波变换算法不但能够很好地去除单分子FRET图像的背景噪声,同时还能很好地保持单分子荧光信号的线性．最后本文还利用滚球算法处理单分子FRET图像及统计15 bp DNA的FRET效率的直方图,通过计算得到了15 bp DNA的FRET效率值．     

小波变换及滚球算法在单分子荧光能量共振转移图像分析中的应用（英文）

单分子荧光共振能量转移技术是通过检测单个分子内的荧光供体及受体间荧光能量转移的效率来研究分子构象的变化.要得到这些生物大分子的信息就需要对大量的单分子信号进行统计分析,人工分析这些信息,既费时费力又不具备客观性和可重复性,因此本文将小波变换及滚球算法应用到单分子荧光能量共振转移图像中对单分子信号进行统计分析.在保证准确检测到单分子信号的前提下,文章对滚球算法和小波变换算法处理图像后的线性进行了分析,结果表明,滚球算法和小波变换算法不但能够很好地去除单分子FRET图像的背景噪声,同时还能很好地保持单分子荧光信号的线性.最后本文还利用滚球算法处理单分子FRET图像及统计15 bp DNA的FRET效率的直方图,通过计算得到了15 bp DNA的FRET效率值.     

基于恒定空间分辨率离散序列小波变换的眼底血管造影图像拼接方法

将恒定空间分辨率离散序列小波变换（discrete sequence wavelet transform,DSWT)应用于眼底吲哚青绿血管造影（indocyanine green angiography,ICGA)图像的拼接,解决了传统基为2的DSWT会导致分解结果的空间分辨率下降的问题。提出对图像小波分解细节逼近和平滑逼近分别使用加权平均拼接和直接平均拼接进行处理的策略,以得到兼顾视觉效果和保真性的拼接结果。并且针对眼底图像背景光照不一致,提出在小波域进行处理的策略。实验结果表明拼接算法效果良好。     

基于多尺度植物种子图像边缘检测算法的设计与实现

小波变换,由于其具有时频局部化的特性及多尺度特性,能敏感地反映突变信号,是一种理想的边缘提取方法．本文系统地介绍了作者在图像边缘检测方面所做的理论探讨、算法及应用研究工作．目前的边缘提取方法有多种,本文将重点集中于基于小波变换的图像边缘检测方法的理论推导和算法实现．     

应用小波变换检测细胞显微荧光图像中的囊泡

文章提出了一种用小波变换来检测生物荧光图像中囊泡的方法。作者用à trous小波对图像进行小波变换,然后求出每层系数的中值绝对偏差σ,并用t=kσ/0.67作为阈值对每层系数进行门限滤波,然后通过提取小波变换系数来重构图像。通过设计实验与常用的“rolling ball”算法对比,发现小波变换算法在低信噪比的情况下,具有更好的灵敏度;对于形状大小不同的信号,具有更好的稳定性;而且对于信号的细节信息具有更好的保真性。     

基于多小波的胃癌病理细胞图像边缘检测与分析

对胃癌细胞图像的多尺度小波变换边缘检测进行了研究,为医生运用现代信息理论的方法进行相关疾病诊断提供了一种新的思路和途径。提出了多尺度小波边缘检测的新方法,归纳了改善小波边缘检测效果的一些策略。实验结果表明,对于具有复杂纹理的医学病理细胞图像,采用传统的边缘检测方法会产生伪边缘和方向性误差,它影响了图像边缘检测的可信度;而运用小波变换的时频尺度特性和对奇异变化的优良检测性能,可得到无噪声污染的图像实际边缘。     

基于小波分析的医学图像的处理

医学图像的好坏直接影响着医生对病情的诊断和治疗,因此利用数字图像处理等技术对医学图像进行有效的处理,已成为医学图像处理研究和开发的一大热点.小波分析是对傅立叶变换的继承和发展,在医学影像领域有着广阔的应用前景.介绍了二维离散小波变换的一般形式,在图像分解的基础上,利用小波分析对医学图像进行去噪和增强处理,能够有效的改善图像质量,有利于医生对病情的诊断和治疗.     

初级视觉的小波表征及其图象压缩效果

初级视觉的Ｇａｂｏｒ函数模型和变换尺度为３是初级视觉处理外界信息的主要特征。在此基础上,由于小波所具有的多分辨特性与视觉处理由粗到细的过程相一致,因而,希望存在一类能够表征这两个初级视觉特征的小波变换。从这点出发,本文先给出了具有变换尺度为３的正交Ｈａａｒ基,而后给出了具有以上两个特征的小波基和小波滤波器。我们将其应用到图象信息的压缩上,着重与传统二进的小波变换图象压缩的效果进行了比较,结果说明具有视觉特征的小波变换能够提供良好的图象压缩效果和主观视觉效果     

基于PET医学图像边缘检测算法的研究

目的:边缘检测在图像处理中至关重要,可被广泛应用于目标区域识别、区域形状检测、图像分割等图像分析领域。边缘是图像中不平稳现象和不规则结构的重要表现,往往携带着图像中的大量信息,并给出图像轮廓。在医学图像三维显示技术中,为了更精确的临床判别需要得到单像素的清晰轮廓,因此我们提出一种新的边缘检测算法。方法:在传统的小波边缘检测的基础上,提出了一种新的边缘算法,即基于小波极大值边缘检测算法,应用模糊算法构造相应的隶属函数,再对得到的极大值进一步筛选。结果:将该算法应用到医学图像中,最终可以得到较清楚的单像素边缘轮廓,实验结果证明了该算法的可行性。结论:运用这种算法处理过的医学图像边缘锐化更好,更清晰,能够为肿瘤的早期识别提供依据,满足医学影像识别的需要。     

初级视觉的小波表征及其图象压缩效果

初级视觉的Ｇａｂｏｒ函数模型和变换尺度为３是初级视觉处理外界信息的主要特征,在此基础上,由于小波所具有的多分辨特性与视觉处理由粗到细的过程相一致,因而,希望存在一类能够表征这两个初高觉特征的小波亦换。从这点出发,本文先给出了具有变换尺度为３的正交Ｈａａｒ基,而后给出了具有以上两个特征的小波基和小波滤波器。     

A guide to accurate fluorescence microscopy colocalization measurements

Biomolecular interactions are fundamental to the vast majority of cellular processes, and identification of the major interacting components is usually the first step toward an understanding of the mechanisms that govern various cell functions. Thus, statistical image analyses that can be performed on fluorescence microscopy images of fixed or live cells have been routinely applied for biophysical and cell biological studies. These approaches measure the fraction of interacting particles by analyzing dual color fluorescence images for colocalized pixels. Colocalization algorithms have proven to be effective, although the dynamic range and accuracy of these measurements has never been well established. Spatial image cross-correlation spectroscopy (ICCS), which cross-correlates spatial intensity fluctuations recorded in images from two detection channels simultaneously, has also recently been shown to be an effective measure of colocalization as well. Through simulations, imaging of fluorescent antibodies adsorbed on glass and cell measurements, we show that ICCS performs much better than standard colocalization algorithms at moderate to high densities of particles, which are often encountered in cellular systems. Furthermore, it was found that the density ratio between the two labeled species of interest plays a major role in the accuracy of the colocalization analysis. By applying a direct and systematic comparison between the standard, fluorescence microscopy colocalization algorithm and spatial ICCS, we show regimes where each approach is applicable, and more importantly, where they fail to yield accurate results.     

Improved spark and ember detection using stationary wavelet transforms

Calcium sparks and embers are localized intracellular events of calcium release in muscle cells studied frequently by confocal microscopy using line-scan imaging. The large quantity of images and large number of events require automatic detection procedures based on signal processing methods. In the past decades these methods were based on thresholding procedures. Although, recently, wavelet transforms were also introduced, they have not become widespread. We have implemented a set of algorithms based on one- and two-dimensional versions of the à trous wavelet transform. The algorithms were used to perform spike filtering, denoising and detection procedures. Due to the dependence of the algorithms on user adjustable parameters, their effect on the efficiency of the algorithm was studied in detail. We give methods to avoid false positive detections which are the consequence of the background noise in confocal images. In order to establish the efficiency and reliability of the algorithms, various tests were performed on artificial and experimental images. Spark parameters (amplitude, full width-at-half maximum) calculated using the traditional and the wavelet methods were compared. We found that the latter method is capable of identifying more events with better accuracy on experimental images. Furthermore, we extended the wavelet-based transform from calcium sparks to long-lasting small-amplitude events as calcium embers. The method not only solved their automatic detection but enabled the identification of events with small amplitude that otherwise escaped the eye, rendering the determination of their characteristic parameters more accurate.     

Automated tracking of muscle fascicle orientation in B-mode ultrasound images

B-mode ultrasound can be used to non-invasively image muscle fascicles during both static and dynamic contractions. Digitizing these muscle fascicles can be a timely and subjective process, and usually studies have used the images to determine the linear fascicle lengths. However, fascicle orientations can vary along each fascicle (curvature) and between fascicles. The purpose of this study was to develop and test two methods for automatically tracking fascicle orientation. Images were initially filtered using a multiscale vessel enhancement (a technique used to enhance tube-like structures), and then fascicle orientations quantified using either the Radon transform or wavelet analysis. Tests on synthetic images showed that these methods could identify fascicular orientation with errors of less than 0.06°. Manual digitization of muscle fascicles during a dynamic contraction resulted in a standard deviation of angle estimates of 1.41° across ten researchers. The Radon transform predicted fascicle orientations that were not significantly different from the manually digitized values, whilst the wavelet analysis resulted in angles that were 1.35° less, and reasons for these differences are discussed. The Radon transform can be used to identify the dominant fascicular orientation within an image, and thus used to estimate muscle fascicle lengths. The wavelet analysis additionally provides information on the local fascicle orientations and can be used to quantify fascicle curvatures and regional differences with fascicle orientation across an image.     

Automated Detection of Soma Location and Morphology in Neuronal Network Cultures

Automated identification of the primary components of a neuron and extraction of its sub-cellular features are essential steps in many quantitative studies of neuronal networks. The focus of this paper is the development of an algorithm for the automated detection of the location and morphology of somas in confocal images of neuronal network cultures. This problem is motivated by applications in high-content screenings (HCS), where the extraction of multiple morphological features of neurons on large data sets is required. Existing algorithms are not very efficient when applied to the analysis of confocal image stacks of neuronal cultures. In addition to the usual difficulties associated with the processing of fluorescent images, these types of stacks contain a small number of images so that only a small number of pixels are available along the z-direction and it is challenging to apply conventional 3D filters. The algorithm we present in this paper applies a number of innovative ideas from the theory of directional multiscale representations and involves the following steps: (i) image segmentation based on support vector machines with specially designed multiscale filters; (ii) soma extraction and separation of contiguous somas, using a combination of level set method and directional multiscale filters. We also present an approach to extract the soma’s surface morphology using the 3D shearlet transform. Extensive numerical experiments show that our algorithms are computationally efficient and highly accurate in segmenting the somas and separating contiguous ones. The algorithms presented in this paper will facilitate the development of a high-throughput quantitative platform for the study of neuronal networks for HCS applications.     

A Novel Dictionary Based Computer Vision Method for the Detection of Cell Nuclei

Cell nuclei detection in fluorescent microscopic images is an important and time consuming task in a wide range of biological applications. Blur, clutter, bleed through and partial occlusion of nuclei make individual nuclei detection a challenging task for automated image analysis. This paper proposes a novel and robust detection method based on the active contour framework. Improvement over conventional approaches is achieved by exploiting prior knowledge of the nucleus shape in order to better detect individual nuclei. This prior knowledge is defined using a dictionary based approach which can be formulated as the optimization of a convex energy function. The proposed method shows accurate detection results for dense clusters of nuclei, for example, an F-measure (a measure for detection accuracy) of 0.96 for the detection of cell nuclei in peripheral blood mononuclear cells, compared to an F-measure of 0.90 achieved by state-of-the-art nuclei detection methods.     

基于独立元分析和联合小波熵检测多导联ECG信号的QRS

QRS波群的准确定位是ECG信号自动分析的基础。为提高QRS检测率,提出一种基于独立元分析（ICA）和联合小波熵（CWS）检测多导联ECG信号QRS的算法。ICA算法从滤波后的多导联ECG信号中分离出对应心室活动的独立元;然后对各独立元进行连续小波变换（CWT）,重构小波系数的相空间,结合相空间中的QRS信息对独立元排序;最后检测排序后独立元的CWS得到QRS信息。实验对St.Petersburg12导联心率失常数据库及64导联犬心外膜数据库测试,比较本文算法与单导联QRS检测算法和双导联QRS检测算法的性能。结果表明,该文算法的性能最好,检测准确率分别为99.98%和100%。